Canonical Allele Identifier: CA2572490199
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056891C>A , CM000665.2:g.53056891C>A GRCh38
NC_000003.11:g.53090907C>A , CM000665.1:g.53090907C>A GRCh37
NC_000003.10:g.53065947C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9652G>T
ENST00000607283.5:c.465-13637G>T
ENST00000607495.5:c.447+20797G>T